The answer from this questions is the letter
B. He should not use his opinions as evidence.
The protons of methylene group between the two carbonyl groups in ethylacetoacetate are acidic in nature. When compounds containing such acidic protons are treated with bases the loose proton and form enolates.
In this particular example when ethylacetoacetate is reacted with methyl magnesium bromide, the methyl group abstracts the acidic proton and converts into
methane gas. The enolate when hydrolyzed is again converted into ethylacetoacetate as shown below,
<h3><u>Answer</u>;</h3>
B.The rate of forward reaction increases.
<h3><u>Explanation;</u></h3>
- Le Chatelier's principle states that changing a factor such as concentration, temperature, or pressure of a reaction at equilibrium will cause the reaction to shift in the direction that counteracts the effect of that change.
- <em><u>Therefore, when reactants are added to a reaction at equilibrium shift when more reactants are added then the reaction shifts to the right to make more products.</u></em>
Answer:
it would be the second one thank me later
Explanation:
Answer:
Their identity changes in both Reaction A and Reaction B.